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Fresenius Kabi USA, LLC recalls The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS). Model Number: LVP-0004.
Recalled June 10, 2026 · FDA recall Z-2274-2026 · Fresenius Kabi USA
Hazard
Potential for the Cassette Loading Lever to break. · FDA Class II
Units
18,444 installed bases
Sold at
US Nationwide distribution in the states of CA, CO, FL, GA, ID, IL, MA, MD, ME, MI, MN, MS, NE, NJ, NV, OK, OR, SC, TX, VA, WA, WI.
Description
Potential for the Cassette Loading Lever to break.
Product
The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS). Model Number: LVP-0004.
Manufacturer(s)
Fresenius Kabi USA, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →